A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3546569



Internal ID22415555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:135147415..135225242hg38UCSC Ensembl
chrX:134281342..134359186hg19UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg3877828
hg1977845
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14467197, nssv14464201, nssv14455305, nssv14456551, nssv14452758
SamplesNA19238, NA19239, HG00731, NA19240, HG00733
Known GenesCXorf48
MethodSequencing
AnalysisSingle strand sequencing, and assortment analysis
PlatformStrand-seq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3546569
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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